共查询到20条相似文献,搜索用时 31 毫秒
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A stereoselective method for the synthesis of substituted tetrahydrofuran derivatives employing a tandem alkylation-Michael addition sequence to vinylogous carbonates is developed. The method could be used to synthesize THFs bearing tertiary ethers. Further, the method is extended to the synthesis of adjacent bis-THFs. 相似文献
3.
A method for the convenient synthesis of phosphonothioates, or phosphonothioic acids, is reported. A significant advantage of the method is the alleviation of the need for purification of intermediates, other than washing with water. No chromatography is needed and the only purification step is the crystallization of the final product. The method uses standard reagents and should be applicable to the synthesis of phosphonothioic acids bearing a range of functional groups. 相似文献
4.
《Journal of fluorine chemistry》1988,40(1):23-32
A convenient method for the synthesis of the previously unknown 2, 6-diformyl-4-trifluoromethylphenol is reported by a seven-stage synthesis. A methyl ether is used to protect the phenol moiety and the key-step involves a copper-mediated trifluoromethylation of a bromoanisole prepared from 4-bromophenol. 相似文献
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A new method is described for palladium-catalyzed allylic silylation using allylic alcohols and disilanes as precursors. The reactions proceed smoothly under mild and neutral conditions, and this method is suitable for synthesis of regio- and stereodefined allylsilanes. The presented silylation reaction can be easily extended to include synthesis of allylboronates by change of the dimetallic reagent. The presented synthetic procedure offers a broad platform for the selective synthesis of functionalized allyl metal reagents, which are useful precursors in advanced organic chemistry and natural product synthesis. 相似文献
6.
Takaoka LR Buckmelter AJ LaCruz TE Rychnovsky SD 《Journal of the American Chemical Society》2005,127(2):528-529
A synthesis of spiroacetals was developed using a reductive cyclization strategy that leads stereoselectively to spiroacetals with a single anomeric stabilization. The method begins with the synthesis of spiro ortho esters. The ortho ester is converted to a cyano acetal. Reductive lithiation of the cyano acetal generates an axial dialkoxylithium reagent, and intramolecular cyclization produces a new ring with retention of configuration. The strategy is convergent and produces complex spiro acetals in only a few steps. The method will be useful in the synthesis of natural products and will facilitate the synthesis of previously inaccessible contra-thermodynamic acetals. 相似文献
7.
微波固相法合成钠快离子导体Na5YSi4O12 总被引:6,自引:0,他引:6
应用微波方法合固相反应难于制备的Na5YSi4O12纯相,讨论了微波合成条件对产物的影响,与溶胶-凝胶法相比,微波法反应速率快,选择性强,合成的样品具有特异的聚集态,缺陷和微结构,从而导致离子导电活化能下降。 相似文献
8.
Stephen Brand John Milton Martin F. Jones Christopher M. Rayner 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):367-368
A new method for the synthesis of cyclic and acyclic optically active S,O-acetals is reported, along with subsequent stereocontrolled transformations, culminating in a synthesis of the important antiviral nucleoside Lamivudine. 相似文献
9.
[reaction: see text] A synthesis of (S,S)-isodityrosine 1, a naturally occurring, key structural subunit of numerous biologically active macromolecules, is described. A formal [3 + 2 + 1] cycloaddition (D?tz benzannulation) approach was utilized to simultaneously construct an aromatic ring and the diaryl ether linkage in one step. This key step was extended to the synthesis of (S,S)-isodityrosine in two separate convergent synthetic routes. This method demonstrates a novel and mild method for the synthesis of diaryl ethers. 相似文献
10.
Lawrence A. Reiter Katherine E. Brighty Rhonda A. Bryant Miriam E. Goldsmith 《合成通讯》2013,43(7):1423-1429
A convenient method for the synthesis of mono N-substituted guanylthioureas in reasonable yields from readily available starting materials has been developed. In contrast to the previously published method, the use of highly noxious hydrogen sulfide is avoided. The method allows the rapid preparation of guanylthioureas since the synthesis of each requires only a single step from a common intermediate, the S-methylated derivative of dithiobiuret. 相似文献
11.
A convenient method for the synthesis of ellipticine is reported. This synthesis is achieved by modifying the processes of Woodward and Sainsburg. The overall yield of this five step synthesis is 12 percent. 相似文献
12.
Stephen Hanessian Stéphane Marcotte Guobin Huang Olivier Loiseleur 《Tetrahedron》2006,62(22):5201-5214
The total synthesis of the bicyclic C-nucleoside malayamycin A is described starting with d-ribonolactone. A new method was developed to obtain preparatively important quantities of β-pseudouridine, which was used as an intermediate. The synthesis of a carba N-nucleoside analogue of malayamycin A is also described. 相似文献
13.
A novel method for transition-metal-free synthesis of 7-azaindoles is developed through a one-pot synthesis involving amination of pyridine N-oxides and intramolecular enamine formation. Remarkable features of the method include simple operation, mild reaction conditions, wide substrate scope, and easily accessible starting materials. 相似文献
14.
Jiang Wang Megan E. Hoerrner Mary P. Watson Daniel J. Weix 《Angewandte Chemie (International ed. in English)》2020,59(32):13484-13489
While ketones are among the most versatile functional groups, their synthesis remains reliant upon reactive and low‐abundance starting materials. In contrast, amide formation is the most‐used bond‐construction method in medicinal chemistry because the chemistry is reliable and draws upon large and diverse substrate pools. A new method for the synthesis of ketones is presented here that draws from the same substrates used for amide bond synthesis: amines and carboxylic acids. A nickel terpyridine catalyst couples N‐alkyl pyridinium salts with in situ formed carboxylic acid fluorides or 2‐pyridyl esters under reducing conditions (Mn metal). The reaction has a broad scope, as demonstrated by the synthesis of 35 different ketones bearing a wide variety of functional groups with an average yield of 60±16 %. This approach is capable of coupling diverse substrates, including pharmaceutical intermediates, to rapidly form complex ketones. 相似文献
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Dr. Jiang Wang Megan E. Hoerrner Prof. Mary P. Watson Prof. Daniel J. Weix 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(32):13586-13591
While ketones are among the most versatile functional groups, their synthesis remains reliant upon reactive and low-abundance starting materials. In contrast, amide formation is the most-used bond-construction method in medicinal chemistry because the chemistry is reliable and draws upon large and diverse substrate pools. A new method for the synthesis of ketones is presented here that draws from the same substrates used for amide bond synthesis: amines and carboxylic acids. A nickel terpyridine catalyst couples N-alkyl pyridinium salts with in situ formed carboxylic acid fluorides or 2-pyridyl esters under reducing conditions (Mn metal). The reaction has a broad scope, as demonstrated by the synthesis of 35 different ketones bearing a wide variety of functional groups with an average yield of 60±16 %. This approach is capable of coupling diverse substrates, including pharmaceutical intermediates, to rapidly form complex ketones. 相似文献
17.
[chemical reaction: see text]. A solid phase approach is presented for the synthesis of azapeptide inhibitors and activity based probes (ABPs) for cysteine proteases. This synthetic method allows the incorporation of diverse reactive warheads linked to different peptide recognition elements. Application of this method to the synthesis of a series of caspase probes is described. 相似文献
18.
A mild, efficient, and practical method for the one-step synthesis of acyl azides from carboxylic acids using bis(2-methoxyethyl)aminosulfur trifluoride is described. The reaction was easily extended to the synthesis of the corresponding nitriles by the inclusion of phosphorous reagents. The method can be applied to the synthesis of optically active nitriles in high yields, and is compatible with fluorous phosphines. 相似文献
19.
J. Gopalakrishnan 《Journal of Chemical Sciences》1984,93(3):421-432
A survey of recent developments in preparative solid state chemistry shows that, with a knowledge of structural chemistry
and reactivity patterns of solids, it is possible to synthesize a variety of new solids possessing novel structures. A distinction
is made between synthesis ofnew solids and synthesis of solids bynew methods. Three new routes to solid state synthesis are recognized: the precursor method, and topochemical methods involving redox
and ion-exchange reactions. The low-temperature topochemical methods enable synthesis of metastable phases that are inaccessible
by the high temperature route. Several illustrative examples of solid state synthesis from the recent literature are presented. 相似文献
20.
《Tetrahedron letters》1986,27(15):1657-1660
A convenient and general method for the synthesis of nucleoside 3′,5′-cyclic phosphorothioates using nucleosides as starting materials is described.A synthesis of nucleoside 3′,5′-cyclic phosphorothioates is described. 相似文献